Canonical Allele Identifier: CA2641326632

Gene: HRH4

Linked Data

• gnomAD v4: 18-24476637-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.24476637G>T , CM000680.2:g.24476637G>T	GRCh38
NC_000018.9:g.22056601G>T , CM000680.1:g.22056601G>T	GRCh37
NC_000018.8:g.20310599G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000256906.5:c.358-110G>T MANE Select	ENSP00000256906.4:n.358-110G>T
ENST00000256906.4:c.358-110G>T	ENSP00000256906.4:n.358-110G>T
ENST00000426880.2:c.194-210G>T	ENSP00000402526.2:n.194-210G>T
NM_001143828.1:c.194-210G>T	NP_001137300.1:n.194-210G>T
NM_001160166.1:c.194-110G>T	NP_001153638.1:n.194-110G>T
NM_021624.3:c.358-110G>T	NP_067637.2:n.358-110G>T
XM_011526133.1:c.357+7686G>T	XP_011524435.1:n.357+7686G>T
NM_021624.4:c.358-110G>T MANE Select	NP_067637.2:n.358-110G>T
NM_001143828.2:c.194-210G>T	NP_001137300.1:n.194-210G>T
NM_001160166.2:c.194-110G>T	NP_001153638.1:n.194-110G>T